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Antibodies

NG2 Recombinant Rabbit monoclonal Antibody

Product Sizes
100μl
£689.00
HA751329-100UL
About this Product
SKU:
HA751329
Application:
Western Blot, Flow Cytometry
Buffer:
PBS (pH7.4).
translate.label.attr.clone:
PSH09-98
Clonality:
Monoclonal
Conjugate:
Non-conjugated
Host:
Rabbit
Immunogen:
Recombinant protein within human NG2 aa 1;301-2;224.
Isotype:
IgG
Molecular Weight:
Predicted band size: 251 kDa
Physical State:
Liquid
Purity:
Protein A affinity purified.
Shipping Conditions:
Blue Ice
Storage Conditions:
Store at +4[o]C after thawing. Aliquot store at -20[o]C. Avoid repeated freeze / thaw cycles.
Supplier:
Huabio
Type:
Antibodies: Monoclonal Antibody
Western blot analysis of NG2 on different lysates with Rabbit anti-NG2 antibody (HA751329) at 1/10;000 dilution. Lane 1: A375 cell lysate Lane 2: SK-MEL-28 cell lysate Lane 3: MCF7 cell lysate (negative) Lane 4: HeLa cell lysate Lane 5: PANC-1 cell lysate Lane 6: MDA-MB-231 cell lysate Lysates/proteins at 20 µg/Lane. Predicted band size: 251 kDa Observed band size: $330 kDa Exposure time: Lane 1-2: 6 seconds; Lane 3-6: 59 seconds; ECL: K1801; 3-8% SDS-PAGE gel. Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (HA751329) at 1/10;000 dilution was used in 5% NFDM/TBST at 4℃ overnight. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1/50;000 dilution was used for 1 hour at room temperature.
Immunocytochemistry analysis of A375 (positive) and SK-Br-3 (negative) labeling NG2 with Rabbit anti-NG2 antibody (HA751329) at 1/100 dilution. Cells were fixed in 4% paraformaldehyde for 15 minutes at room temperature; permeabilized with 0.1% Triton X-100 in PBS for 15 minutes at room temperature; then blocked with 1% BSA in 10% negative goat serum for 1 hour at room temperature. Cells were then incubated with Rabbit anti-NG2 antibody (HA751329) at 1/100 dilution in 1% BSA in PBST overnight at 4 ℃. Goat Anti-Rabbit IgG H&L (iFluor™ 488; HA1121) was used as the secondary antibody at 1/1;000 dilution. PBS instead of the primary antibody was used as the secondary antibody only control. Nuclear DNA was labelled in blue with DAPI. Beta tubulin (HA601187; red) was stained at 1/100 dilution overnight at +4℃. Goat Anti-Mouse IgG H&L (iFluor™ 594; HA1126) was used as the secondary antibody at 1/1;000 dilution.
Flow cytometric analysis of SK-Br-3 (left; negative) and A375 (right; positive) cells labeling NG2. Cells were fixed and permeabilized. Then stained with the primary antibody (HA751329; 1/1;000) (red) compared with Rabbit IgG Isotype Control (green). After incubation of the primary antibody at +4℃ for an hour; the cells were stained with a iFluor™ 488 conjugate-Goat anti-Rabbit IgG Secondary antibody (HA1121) at 1/1;000 dilution for 30 minutes at +4℃. Unlabelled sample was used as a control (cells without incubation with primary antibody; black).